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A Signature of Three microRNAs Is a Potential Diagnostic Biomarker for Glioblastoma
BACKGROUND: Glioblastoma is the most common primary malignant neoplasm of the central nervous system. Despite progress in diagnosis and treatment, glioblastoma still has a poor prognosis. This study aimed to examine whether a signature of three candidate miRNAs (i.e. hsa-let-7c-5p, hsa-miR-206-5p, a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pasteur Institute of Iran
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9432466/ https://www.ncbi.nlm.nih.gov/pubmed/35490305 http://dx.doi.org/10.52547/ibj.3671 |
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author | Yazdi, Ali Hosein Zarrinpour, Vajiheh Moslemi, Elham Forghani Fard, Mohamad Mahdi |
author_facet | Yazdi, Ali Hosein Zarrinpour, Vajiheh Moslemi, Elham Forghani Fard, Mohamad Mahdi |
author_sort | Yazdi, Ali Hosein |
collection | PubMed |
description | BACKGROUND: Glioblastoma is the most common primary malignant neoplasm of the central nervous system. Despite progress in diagnosis and treatment, glioblastoma still has a poor prognosis. This study aimed to examine whether a signature of three candidate miRNAs (i.e. hsa-let-7c-5p, hsa-miR-206-5p, and hsa-miR-1909-5p) can be used as a diagnostic biomarker for distinguishing glioblastoma from healthy brain tissues. METHODS: In this study, 50 FFPE glioblastoma tissue samples and 50 healthy tissue samples adjacent to tumor were included. The expression of each candidate miRNA (i.e. hsa-let-7c-5p, hsa-miR-206-5p, and hsa-miR-1909-5p) was measured using RT-qPCR. To show the roles of each miRNA and their biological effects on glioblastoma development and clinicopathological characteristics, in silico tools were used. ROC curves were performed to assess the diagnostic accuracy of each miRNA. RESULTS: Based on the results, hsa-let-7c-5p and hsa-miR-206-5p were downregulated, while hsa-miR-1909-5p was upregulated in glioblastoma tumors compared to healthy samples. No association was detected between the expression of each candidate miRNA and sex. Except for hsa-let-7c-5p, other miRNAs did not correlate with age status. ROC curve analysis indicated that the signature of candidate miRNAs is a potential biomarker distinguishing between glioblastoma and healthy samples. Only hsa-miR-206-5p suggested the association with poor prognosis in glioblastoma patients. CONCLUSION: Our findings revealed that the signature of three miRNAs is capable of distinguishing glioblastoma tumor and healthy tissues. These results are beneficial for the clinical management of glioblastoma patients. |
format | Online Article Text |
id | pubmed-9432466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Pasteur Institute of Iran |
record_format | MEDLINE/PubMed |
spelling | pubmed-94324662022-09-13 A Signature of Three microRNAs Is a Potential Diagnostic Biomarker for Glioblastoma Yazdi, Ali Hosein Zarrinpour, Vajiheh Moslemi, Elham Forghani Fard, Mohamad Mahdi Iran Biomed J Full Length BACKGROUND: Glioblastoma is the most common primary malignant neoplasm of the central nervous system. Despite progress in diagnosis and treatment, glioblastoma still has a poor prognosis. This study aimed to examine whether a signature of three candidate miRNAs (i.e. hsa-let-7c-5p, hsa-miR-206-5p, and hsa-miR-1909-5p) can be used as a diagnostic biomarker for distinguishing glioblastoma from healthy brain tissues. METHODS: In this study, 50 FFPE glioblastoma tissue samples and 50 healthy tissue samples adjacent to tumor were included. The expression of each candidate miRNA (i.e. hsa-let-7c-5p, hsa-miR-206-5p, and hsa-miR-1909-5p) was measured using RT-qPCR. To show the roles of each miRNA and their biological effects on glioblastoma development and clinicopathological characteristics, in silico tools were used. ROC curves were performed to assess the diagnostic accuracy of each miRNA. RESULTS: Based on the results, hsa-let-7c-5p and hsa-miR-206-5p were downregulated, while hsa-miR-1909-5p was upregulated in glioblastoma tumors compared to healthy samples. No association was detected between the expression of each candidate miRNA and sex. Except for hsa-let-7c-5p, other miRNAs did not correlate with age status. ROC curve analysis indicated that the signature of candidate miRNAs is a potential biomarker distinguishing between glioblastoma and healthy samples. Only hsa-miR-206-5p suggested the association with poor prognosis in glioblastoma patients. CONCLUSION: Our findings revealed that the signature of three miRNAs is capable of distinguishing glioblastoma tumor and healthy tissues. These results are beneficial for the clinical management of glioblastoma patients. Pasteur Institute of Iran 2022-07 2022-08-07 /pmc/articles/PMC9432466/ /pubmed/35490305 http://dx.doi.org/10.52547/ibj.3671 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Length Yazdi, Ali Hosein Zarrinpour, Vajiheh Moslemi, Elham Forghani Fard, Mohamad Mahdi A Signature of Three microRNAs Is a Potential Diagnostic Biomarker for Glioblastoma |
title | A Signature of Three microRNAs Is a Potential Diagnostic Biomarker for Glioblastoma |
title_full | A Signature of Three microRNAs Is a Potential Diagnostic Biomarker for Glioblastoma |
title_fullStr | A Signature of Three microRNAs Is a Potential Diagnostic Biomarker for Glioblastoma |
title_full_unstemmed | A Signature of Three microRNAs Is a Potential Diagnostic Biomarker for Glioblastoma |
title_short | A Signature of Three microRNAs Is a Potential Diagnostic Biomarker for Glioblastoma |
title_sort | signature of three micrornas is a potential diagnostic biomarker for glioblastoma |
topic | Full Length |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9432466/ https://www.ncbi.nlm.nih.gov/pubmed/35490305 http://dx.doi.org/10.52547/ibj.3671 |
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